Abstract
We treated a Japanese man with Rendu-Osler-Weber disease and a recurrent encephalopathy with hyperammonemia concomitant with recurrent epistaxis, G-I bleeding, congestive heart failure with aortic and mitral regurgitation, and chronic renal failure. At peritoneoscopy, several telangiectasia were noted on the surface of the liver. Angiographical studies revealed widened and tortuous hepatic arteries with early filling of hepatic veins and small pools of contrast medium scattered throughout the parenchyma. The recurrent encephalopathy was attributed to the porto-systemic shunt formed in the liver. © 1987, The Japanese Society of Internal Medicine. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
Okabe, H., Ishibashi, H., Kimura, H., Yokota, E., Kameda, S., Miyanaga, O., & Niho, Y. (1987). Rendu-Osler-Weber Disease with Portosystemic Encephalopathy. Japanese Journal of Medicine, 26(3), 396–400. https://doi.org/10.2169/internalmedicine1962.26.396
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.